Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,553 recalls have been distributed to Wyoming in the last 12 months.
Showing 4441–4460 of 27,462 recalls
Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...
The Issue: The expiration date was not printed on the outer shipping label, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...
The Issue: The expiration date was not printed on the outer shipping label, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...
The Issue: The expiration date was not printed on the outer shipping label, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Anti-HCV Reagent Kit Recalled by Abbott GmbH Due to Customer...
The Issue: Customer complaints were received regarding falsely elevated results for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Guide Handpiece Adaptor Sleeve 1 Recalled by X-NAV Technologies, LLC Due...
The Issue: The Handpiece Adaptor may have a manufacturing defect causing incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Guide Handpiece Adaptor Sleeve 3 Recalled by X-NAV Technologies, LLC Due...
The Issue: The Handpiece Adaptor may have a manufacturing defect causing incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Anti-HCV Reagent Kit Recalled by Abbott GmbH Due to Customer...
The Issue: Customer complaints were received regarding falsely elevated results for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iQ 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update to...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo Full Face with Headgear Recalled by SleepNet Corporation Due to Update...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phantom 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo 2 Full Face Non Vented Mask Recalled by SleepNet Corporation Due to...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo 2 Full Face Vented Mask Recalled by SleepNet Corporation Due to Update...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo 2 Full Face AAV Non Vented Mask Recalled by SleepNet Corporation Due to...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo Non Vented Full Face Mask with Headgear Recalled by SleepNet...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entuit Secure Adjustable Gastrointestinal Suture Anchor Set - Intended for...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25-LHP-828 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...
The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25-LHP-928 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...
The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N-LHP-928 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...
The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dilator - Coons Taper - Used for dilating puncture sites Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dilator - Intended to be used for dilating puncture sites Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.